US4112740A - Method and apparatus for determining a change of the flow state of flowable substances from its static state to its flowing state or vice verse - Google Patents
Method and apparatus for determining a change of the flow state of flowable substances from its static state to its flowing state or vice verse Download PDFInfo
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- US4112740A US4112740A US05/816,715 US81671577A US4112740A US 4112740 A US4112740 A US 4112740A US 81671577 A US81671577 A US 81671577A US 4112740 A US4112740 A US 4112740A
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N29/00—Investigating or analysing materials by the use of ultrasonic, sonic or infrasonic waves; Visualisation of the interior of objects by transmitting ultrasonic or sonic waves through the object
- G01N29/44—Processing the detected response signal, e.g. electronic circuits specially adapted therefor
- G01N29/449—Statistical methods not provided for in G01N29/4409, e.g. averaging, smoothing and interpolation
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N29/00—Investigating or analysing materials by the use of ultrasonic, sonic or infrasonic waves; Visualisation of the interior of objects by transmitting ultrasonic or sonic waves through the object
- G01N29/02—Analysing fluids
- G01N29/032—Analysing fluids by measuring attenuation of acoustic waves
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N29/00—Investigating or analysing materials by the use of ultrasonic, sonic or infrasonic waves; Visualisation of the interior of objects by transmitting ultrasonic or sonic waves through the object
- G01N29/34—Generating the ultrasonic, sonic or infrasonic waves, e.g. electronic circuits specially adapted therefor
- G01N29/346—Generating the ultrasonic, sonic or infrasonic waves, e.g. electronic circuits specially adapted therefor with amplitude characteristics, e.g. modulated signal
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N29/00—Investigating or analysing materials by the use of ultrasonic, sonic or infrasonic waves; Visualisation of the interior of objects by transmitting ultrasonic or sonic waves through the object
- G01N29/34—Generating the ultrasonic, sonic or infrasonic waves, e.g. electronic circuits specially adapted therefor
- G01N29/348—Generating the ultrasonic, sonic or infrasonic waves, e.g. electronic circuits specially adapted therefor with frequency characteristics, e.g. single frequency signals, chirp signals
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N29/00—Investigating or analysing materials by the use of ultrasonic, sonic or infrasonic waves; Visualisation of the interior of objects by transmitting ultrasonic or sonic waves through the object
- G01N29/36—Detecting the response signal, e.g. electronic circuits specially adapted therefor
- G01N29/40—Detecting the response signal, e.g. electronic circuits specially adapted therefor by amplitude filtering, e.g. by applying a threshold or by gain control
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N29/00—Investigating or analysing materials by the use of ultrasonic, sonic or infrasonic waves; Visualisation of the interior of objects by transmitting ultrasonic or sonic waves through the object
- G01N29/36—Detecting the response signal, e.g. electronic circuits specially adapted therefor
- G01N29/42—Detecting the response signal, e.g. electronic circuits specially adapted therefor by frequency filtering or by tuning to resonant frequency
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/483—Physical analysis of biological material
- G01N33/487—Physical analysis of biological material of liquid biological material
- G01N33/49—Blood
- G01N33/4905—Determining clotting time of blood
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2291/00—Indexing codes associated with group G01N29/00
- G01N2291/02—Indexing codes associated with the analysed material
- G01N2291/028—Material parameters
- G01N2291/02836—Flow rate, liquid level
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2291/00—Indexing codes associated with group G01N29/00
- G01N2291/10—Number of transducers
- G01N2291/102—Number of transducers one emitter, one receiver
Definitions
- the present invention relates to a new and improved method of, and apparatus for, determining a change of the flow state or condition of a flowable or fluent substance by means of ultrasonic energy or ultrasound.
- the method for determining the change of such flow state contemplates transmitting ultrasonic or ultrasound waves of substantially constant frequency to a spatial region or specified volume of the substance, receiving the ultrasonic waves which are backscattered by the substance, converting the same into an amplitude- and phase-modulated primary signal corresponding to the backscattering and demodulating the primary signal in order to obtain a modulation signal which can be divided into a spectrum of signal components of different frequency and possessing pseudo periods which are defined as the time spacing between successive momentary values of the modulation signal and corresponding to one another.
- the apparatus for determining the flow condition of a fluent or flowable substance is of the type comprising a signal generator for generating a reference signal of substantially constant frequency, an ultrasonic transmitter arranged in series with the signal generator for transmitting ultrasonic waves corresponding to the reference signal to a spatial region or specified volume of the substance. Further, there is provided an ultrasonic receiver for receiving ultrasonic or ultrasound waves backscattered at the substance and for converting the same into an amplitude- and phase-modulated primary signal corresponding to the backscattering.
- a demodulator serves for obtaining a modulation signal from the primary signal and an analyser serves for detecting signal components of the modulation signal.
- the measured intensity is essentially constant, its value corresponds to the backscattering of the ultrasonic waves by the static or stationary sample liquid and therefore does not amount to null.
- the intensity of the backscattered ultrasonic waves fluctuates about a mean value.
- Still a further significant object of the present invention aims at the provision of a new and improved construction of apparatus for determining a change of the flow state of a flowable material or substance in an extremely accurate, relatively simple and reliable manner, which apparatus is easy to use, economical to construct, highly reliable in operation, and not readily subject to malfunction or breakdown.
- Yet a further object of this invention is to provide a novel method of determining a change of the flow state or condition of a flowable substance with greater accuracy than heretofore possible, while eliminating the drawbacks of the prior art proposal discussed above.
- the method of the present development for determining a change of the flow state of a flowable substance importantly contemplates the step of comparing the time duration corresponding to a predetermined number of pseudo periods with a predetermined time duration.
- the invention is further concerned with apparatus useful for the performance of the aforesaid method, which apparatus contemplates structuring the analyser to possess a detector which always then delivers a detector signal upon the occurrence of a predetermined momentary value of the modulation signal.
- a pulse generator is arranged following the detector, the pulse generator always then delivering a predetermined pulse upon receiving a detector signal.
- the analyser further comprises at least one analyser device which is arranged following the pulse generator, the analyser device containing an integrator having charging- and discharging-time constants and a comparator arranged after such integrator.
- the analyser device serves for the integration of a pulse sequence or train formed of the pulses, for comparing the result of the integration with a predetermined threshold value and for delivering an analyser signal upon the presence of a predetermined result of such comparison.
- FIG. 1 schematically illustrates a constructional embodiment of apparatus for the determination of the flow state or condition of a substance
- FIG. 2 is a schematic block circuit diagram of the analyser illustrated in the arrangement of FIG. 1;
- FIG. 3 portrays charge curves of the integrator illustrated in FIG. 2;
- FIG. 4 is a block circuit diagram of a modified embodiment of analyser.
- FIG. 5 schematically illustrates a block circuit diagram of a variant embodiment from that shown in FIG. 1.
- a sample container 1 for housing a flowable or fluent substance 2, the flow state of which is to be ascertained.
- This substance 2 can be for instance whole blood contained in a cuvette or vial or the like, and it can be assumed that there is to be ascertained whether the whole blood is coagulating or coagulated.
- the teachings of the invention are not limited to blood or like substances, and specifically it is to be understood that the same can also process substances which are flowable but not liquid, for instance fluidized solids employed in the chemical industry in a turbulent bed reactor, where for instance there is to be detected whether the fluidized solids are present, i.e. whether gas and solid particles form a turbulent, microscopic inhomogeneous yet macroscopic homogeneous mixture or whether there has settled a stationary layer of solid particles.
- there are processed substances possessing microscopic inhomogeneities the distribution of which, considered macroscopically, can be homogeneous or inhomogeneous or can possess a static state and a moving state.
- an ultrasonic transmitter or transducer 3 is arranged at the container 1.
- a signal generator 4 produces a reference signal of constant frequency for controlling the transmitter 3, the reference signal being delivered to the ultrasonic or ultrasound transmitter 3 by means of a line or conductor 5.
- the ultrasonic or ultrasound transmitter or transducer 3 produces a beam of ultrasonic waves which have been merely conveniently symbolized by the squiggly or undulated arrow 6, whereas the beam has been symbolically delimited by the broken lines 7 and 8.
- An ultrasonic or ultrasound receiver 9 is arranged at the container 1 in such a manner that it is impinged by the ultrasonic or ultrasound waves, symbolized by the undulated arrow 10, backscattered by the substance 2, however not by the transmitted ultrasonic waves 6.
- the ultrasonic receiver 9 delivers a primary signal by means of an output line or conductor 11.
- the reference signal is thus converted into transmitted ultrasonic waves, and the backscattered ultrasonic waves are converted into the primary signal.
- the necessary measures for coupling the ultrasonic transmitter or transducer 3 and the receiver 9 with the substance 2 by means of the container 1 are well known in the art and therefore need not be further considered in this disclosure.
- the reference signal and the primary signal are electrical signals, the infeed and outfeed of which requires the use of conventional matching techniques such as impedance transformation or conversion, amplification and the like, which likewise need not be here further considered since these techniques are well known in the electronics art. It is however to be mentioned that the invention is not in principle limited to electrical signals provided that other type of signals or other type of signal transmission can be used, which, for instance, fall into the fields of optical, acoustical or mechanical technology.
- the backscattering of the ultrasonic waves 6 due to the inhomogeneities of the substance 2 is governed by statistical laws: the primary signal is amplitude- and phase-modulated in accordance with the backscattering. If the substance 2 is at a state of rest, i.e. static, then the modulation is equal to null.
- the Brownian motion and convection: particle suspensions, emulsions and the like therefore can cause a modulation of the primary signal even in a "static state", yet such primary signal as concerns its amplitude and frequency possesses a spectrum which differs from the spectrum associated with a moving state of the sample or substance.
- the demodulator 12 is a phase detector to which there is delivered by means of the line 11 the primary signal and by means of a not particularly referenced branched-off portion of the line or conductor 5 the reference signal.
- a particularly advantageous constructional embodiment of demodulator 12 as a phase detector comprises a dual-gate MOS-FET, which is supplied by a respective signal from the lines or conductors 5 and 11.
- Such dual-gate MOS-FET circuitry is well known in the art and thus need not be here further considered. It also would be possible to carry out, instead of the here performed phase modulation, an amplitude modulation and to likewise process such obtained signal in a manner as will be considered in the description to follow.
- the modulation signal delivered at the output of the demodulator 12 to the line or conductor 13 is fed to an analyser 14.
- the analyser 14 there is initially determined the time duration needed for a predetermined number of pseudo periods of the modulation signal, this being equivalent to the mean frequency of the spectrum of the modulation signal. Thereafter an analyser signal is supplied to an output line 15 of the analyser 14 when the determined time duration has exceeded a predetermined time duration or, selectively, falls below a predetermined time duration. In conventional manner this can be accomplished by comparison of the counter state of counters for the pseudo periods and the time pulses.
- other particularly favorable constructions will be considered.
- FIG. 2 One particularly favorable constructional embodiment of the analyser 14 of the apparatus of FIG. 1 has been shown in greater detail in FIG. 2 where the lines or conductors 13 and 15 of FIG. 1 have been illustrated.
- the modulation signal is fed by means of the line 13 to a detector 20 which delivers a detector signal through a line or conductor 21 when the modulation signal has reached a predetermined momentary value.
- the detector 20 is constructed for instance as a Schmitt-trigger operating as a null value detector, this Schmitt-trigger delivering a detector signal when the modulation signal possesses a null throughpass from a negative to a positive value.
- the operating point of the Schmitt-trigger can be shifted in conventional manner.
- the detector 20 a conventional peak value detector in order to produce the detector signal when the modulation signal has reached a maximum or, selectively, a minimum.
- the detector signal is delivered by the line or conductor 21 to a pulse generator 22 which always then delivers a pulse to a line or conductor 23 when there is infed a detector signal. Both the amplitude as well as the duration of each pulse is predetermined, and thus there is formed a pulse sequence or train of successively identical pulses.
- the duration of the pulses is selected such that it is much shorter than the duration of the pseudo periods, the presence of which in the modulation signal is to be evaluated. In the case of short pseudo periods there is in fact only detected the presence thereof, the evaluation being saturated thus furnishes a maximum occurrence rate, because the time spacing of the pulses is vanishingly small. In the normal instance, where the spacing between the pulses is considerably greater than the duration of a pulse, the number of pulses produced during a predetermined time duration constitutes a mean value of the frequencies which arise in the frequency spectrum of the modulation signal.
- the described apparatus also fulfills the purpose of eliminating any effect of the amplitude of the signal components upon the evaluation.
- the pulse sequence or train is supplied to an integrator 24 which possesses both a charging-time constant as well as also a self-discharging time constant.
- the signals at one input 25 and at one output 26 of the integrator 24 are both defined with regard to the ground potential.
- a resistor 27 is connected in circuit between the input 25 and the output 26, while a resistor 28 and a capacitor 29 are connected in parallel between the output 26 and ground.
- the charging-time constant is equal to the product of the value of the resistor 27 and the capacitor 29, whereas the self-discharging time constant is equal to the product of the value of the resistor 28 and the capacitor 29.
- FIG. 3 there is schematically graphically portrayed the course of the voltage V 26 at the output of the integrator 24 as a function of the time t.
- the charging time constant T 1 has been graphically illustrated as well as a respective self-discharging time constant T 2A and T 2B related to an associated curve A and B respectively.
- T 1 a pulse train is infed to the integrator 24, this pulse train comprising a series of pulses, the amplitude of which is assumed to be equal to a value of 100%, and which furthermore contains during the time constant T 1 5 pulses and 5 pulse pauses or intervals of the same duration T 1 /10.
- Such would correspond to a modulation signal which only contains the signal components of the frequency 5/T 1 .
- the voltage V 26 reaches a constant mean or average value during the course of the time, which mean value fluctuates in cycle with the pulses.
- the threshold value is set at 66% of the pulse amplitude, then such threshold value will be exceeded by the curve B after 12 pulses, and will never be exceeded by the curve A.
- an increase of the repetition frequency of the pulses brings about a shortening of the time sections during which the capacitor 29 can discharge and the voltage V 26 can drop. Consequently, the capacitor 29 is charged more quickly and the corresponding charging curve is disposed above the curve B. If the pulses follow one another practically without any pulse gaps, then the charging curve transforms into an exponential charging curve.
- the one time duration is the mean time duration of pseudo periods and can equally be considered as the time duration corresponding to a predetermined number of pseudo periods of the modulation signal, while the other time duration is governed by the selection of the pulse duration and both of the time constants and therefore itself can be considered as predetermined.
- the determination of a frequency mean value which can be achieved with this construction is indeed not as precise as an actual counting of pseudo periods during a counted-off time, but it is however completely sufficient for the determination of the flow state and can be achieved with extreme equipment economies.
- the analyser 14 is to be provided with such characteristic values so that by means thereof there can be accomplished exceeding of the threshold value by the charging state of the integrator by relatively high-frequency signal components of the modulation signal, not however by relatively low-frequency signal components. For instance, in the case of whole blood and plasma there can be selected characteristic values for which there are required 50 pulses in 0.5 seconds in order to produce an analyser signal.
- the static sample liquid then does not produce any analyser signal, whereas an injection of thrombin solution causes turbulence and triggers the analyser signal.
- the analyser In order to determine the point in time at which the substance 2 transforms from a flow state into a static state, the analyser should be equipped with characteristic values for obtaining the reverse mode of operation or function. With coagulated whole blood or plasma not only does there disappear the turbulence and the convection, but also part of the Brownian movement. If additionally, as described more fully hereinafter, in order to suppress disturbing influences there are suppressed low-frequency signal components below approximately 3 Hz, then the analyser signal should be triggered when no pulse has arrived during a predetermined time duration.
- the integrator is to be provided with a charging time constant which is in the same order of magnitude as the pulse duration, so that each pulse charges the integrator to a value exceeding the threshold value.
- the predetermined time duration in this case amounts to the time duration needed for the discharge of the integrator from the charging value to the threshold value, for instance 0.5 seconds.
- FIG. 4 An advantageous constructional embodiment of appropriate apparatus has been shown in FIG. 4 where the same components or elements 13, 20, 21, 22 and 23 have been illustrated as in the arrangement of FIG. 2.
- the null value detector 20 which controls, by means of the line 21, the pulse generator 22 during each similar null throughpass of the modulation signal, so that the line or conductor 23 carries a pulse sequence or train which corresponds to the modulation signal.
- the integrator 24A and 24B each of which possess the same structure as the integrator 24 of the arrangement of FIG. 2 previously discussed. However, there are needed approximately 50 pulses in 0.5 seconds in order to charge the integrator 24A to 66% of a pulse amplitude, whereas the integrator 24B can be charged by a single pulse to approximately 63% of the pulse amplitude. Both integrators discharge by about 63% in 1 second.
- the integrators 24A and 24B are each provided with an output line or conductor 30A and 30B, respectively, which supplies the charging state of the corresponding integrator to a respective input 40A and 40B of a dual or two-fold comparator 41.
- the comparator 41 is a commercially available component having an output 42. This output 42 does not carry any voltage thereat at the the start of the operation, but at the moment when the voltage infed to the input 40A exceeds a first threshold value of 66% of a pulse amplitude then the output 42 carries a voltage, and specifically for such length of time until the voltage delivered to the input 40B falls below a second threshold value of 33% of a pulse amplitude, whereafter the voltage at the output 42 again drops to null.
- the voltage at the output 42 forms an analyser signal which is delivered by the line 43 to a time counter 44 and controls the latter. There is measured the time during which a voltage is carried by the line or conductor 43. It will be apparent that the time count starts as soon as approximately 50 pulses have been produced in 0.5 seconds, and the time count terminates when no pulse has been produced in about 0.5 seconds. Both of the time delays of about 0.5 seconds upon starting and stopping the time count extensively compensate one another, and additionally there exists the possibility of delivering to the time counter a correction value which by far enables obtaining the necessary precision of the measuring technique.
- FIG. 5 there is illustrated a constructional variant of the apparatus shown in FIG. 1 having a sampling circuit for the modulation signal.
- the modulation signal must be sampled when the ultrasonic transmitter or transducer is controlled in its pulse mode or operation, for instance for protecting the transmitter at high intensities or for using the same transducer for transmitting and receiving.
- a synchronization of the sampling with the rhythm or cycle of the ultrasound or ultrasonic pulses renders possible a selective evaluation of the backscattering of the ultrasound waves and thus an examination of a predetermined and spatially limited region or specified volume of the substance.
- FIG. 5 there have been shown components of the arrangement of FIG. 1.
- the conductor or line 13 between the phase detector 12 and the analyser 14 is replaced in the arrangement of FIG. 5 by two lines or conductors 50 and 51.
- the line 50 interconnects the output of the phase detector 12 with an input of a sampling circuit 52 which is conventional in construction and basically functions like a switch which is closed only during short, periodic repetitive time sections and thus connects the line 50 with a line 53.
- a sampling circuit 52 which is conventional in construction and basically functions like a switch which is closed only during short, periodic repetitive time sections and thus connects the line 50 with a line 53.
- This sequence of sampling values is delivered by means of a filter 54 to the line 51 and thus infed to the analyser 14.
- the sampling frequency i.e.
- the rhythm or cycle of the sampling operation is controlled by a control device 55, which, for this purpose, is connected by means of a line or conductor 56 with the sampling circuit 52.
- the control device 55 is also furthermore connected by means of a line 57 with the signal generator 4 in order to control such in its pulse mode.
- the pulses of the ultrasonic or ultrasound waves are synchronized with the rhythm of the sampling operation in such a manner that the sampling values of the phase modulation correspond to an exactly predetermined transit time of the ultrasonic waves, i.e. a spatially limited region of the substance to be examined.
- the filter 54 is a bandpass filter which, on the one hand, suppresses the sampling frequency and, on the other hand, suppresses constant remaining, sampling values.
- the bandpass filter 54 is equipped with a respective lower boundary frequency and an upper boundary frequency. For instance, during a pulse mode and a sampling frequency of 2000 Hz the lower boundary frequency can be set at about 3 Hz and the upper boundary frequency at about 300 Hz. There then appears at the line 51, at the output of the filter 54, a modulation signal, the time course of which is an envelope of the sampling values of the phase modulation, and constant or slow changing values are suppressed.
- the indicated boundary frequencies are especially suitable for the determination of the coagulation time of whole blood.
- the upper boundary value is high enough in order to ensure for an unambiguous differentiation between the liquid and the coagulated state, whereas it is also low enough in order to eliminate with certainty, with technically acceptable values of the pulse duration and the integrator time constants, a saturation of the evaluation.
- the lower boundary value is low enough in order to still render possible the detection of the Brownian movement and/or the convection, whereas it is also high enough in order to avoid disturbances in the analysis by external effects, such as slight jarring of the instrument due to movements of the operator, noise from the surroundings or street and the like. Additionally, the suppression of frequencies below the lower boundary value also allows for the suppression of signals which remain constant, caused for instance by echoes at the walls of the container 1 or by electrical crosstalk between the transmitter and the receiver.
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Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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CH392/77 | 1977-01-13 | ||
CH39277A CH610111A5 (da) | 1977-01-13 | 1977-01-13 |
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US05/816,715 Expired - Lifetime US4112740A (en) | 1977-01-13 | 1977-07-18 | Method and apparatus for determining a change of the flow state of flowable substances from its static state to its flowing state or vice verse |
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US (1) | US4112740A (da) |
JP (1) | JPS5389785A (da) |
AT (1) | AT357807B (da) |
BE (1) | BE857638A (da) |
CA (1) | CA1074002A (da) |
CH (1) | CH610111A5 (da) |
DE (1) | DE2732622C3 (da) |
FR (1) | FR2377628A1 (da) |
GB (1) | GB1594891A (da) |
IT (1) | IT1088792B (da) |
NL (1) | NL7708036A (da) |
SE (1) | SE438913B (da) |
SU (1) | SU689630A3 (da) |
Cited By (16)
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US4357603A (en) * | 1980-11-24 | 1982-11-02 | The United States Of America As Represented By The Depart Of Energy | Method and apparatus for acoustically monitoring the flow of suspended solid particulate matter |
WO1989004482A1 (en) * | 1987-11-02 | 1989-05-18 | Stephan Dymling | Acoustic method for measuring properties of a mobile medium |
WO1995006919A1 (en) * | 1993-08-31 | 1995-03-09 | Boehringer Mannheim Corporation | Method and apparatus for operating a medical instrument |
US5686659A (en) * | 1993-08-31 | 1997-11-11 | Boehringer Mannheim Corporation | Fluid dose flow and coagulation sensor for medical instrument |
US5824881A (en) * | 1996-09-13 | 1998-10-20 | Cobe Laboratories | Gas/fluid detector for contained fluid systems |
US20050148899A1 (en) * | 2003-10-22 | 2005-07-07 | Walker William F. | Method and apparatus for characterization of clot formation |
US9031701B2 (en) | 2011-02-15 | 2015-05-12 | Hemosonics Llc | Characterization of blood hemostasis and oxygen transport parameters |
US9272280B2 (en) | 2011-02-15 | 2016-03-01 | Hemosonics Llc | Device, systems and methods for evaluation of hemostasis |
US20160334371A1 (en) * | 2014-08-08 | 2016-11-17 | Peter Ganshorn | Method and device for determining the proportion of molecular oxygen in a respiratory gas by means of sound |
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US10147152B2 (en) | 2010-04-08 | 2018-12-04 | Hemosonics, Llc | Hemostatic parameter display |
US10996230B2 (en) | 2008-12-23 | 2021-05-04 | C A Casyso Gmbh | Cartridge device for a measuring system for measuring viscoelastic characteristics of a sample liquid, a corresponding measuring system, and a corresponding method |
US11054396B2 (en) | 2011-05-19 | 2021-07-06 | Hemosonics Llc | Hemostasis analyzer |
US11327069B2 (en) | 2014-09-29 | 2022-05-10 | Ca Casyso Gmbh | Blood testing system and method |
US11366093B2 (en) | 2017-04-20 | 2022-06-21 | Hemosonics, Llc | Disposable system for analysis of hemostatic function |
US12031993B2 (en) | 2014-09-29 | 2024-07-09 | C A Casyso Gmbh | Blood testing system and method |
Families Citing this family (4)
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---|---|---|---|---|
FI82776C (fi) * | 1985-04-04 | 1991-04-10 | Kajaani Electronics | Foerfarande och anlaeggning foer analysering av massa. |
JPH088920B2 (ja) * | 1990-09-28 | 1996-01-31 | 富士通株式会社 | 血液散乱パワ用算出装置 |
DE19813975C2 (de) * | 1998-03-20 | 2000-06-15 | Ralf Steger | Verfahren und Einrichtung zum Bestimmen einer rheologischen Kenngröße eines Fluids |
EP3844530A4 (en) | 2018-08-30 | 2022-04-20 | Atomic Energy of Canada Limited/ Énergie Atomique du Canada Limitée | CONTINUOUS ULTRASONIC OR ACOUSTIC NON-DESTRUCTIVE TESTING |
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US3925773A (en) * | 1973-08-31 | 1975-12-09 | Emergency Products Corp | Alarm signal processing system and method |
US4003045A (en) * | 1975-10-01 | 1977-01-11 | Napco Security Systems, Inc. | Intrusion detection systems with turbulence discrimination |
US4012730A (en) * | 1974-03-25 | 1977-03-15 | David Nicholls | Doppler detection device with integrator sampling means to inhibit false alarms |
US4014650A (en) * | 1975-04-25 | 1977-03-29 | Research Corporation | Ultrasonic coagulation timer |
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1977
- 1977-01-13 CH CH39277A patent/CH610111A5/xx not_active IP Right Cessation
- 1977-07-06 AT AT483877A patent/AT357807B/de not_active IP Right Cessation
- 1977-07-18 US US05/816,715 patent/US4112740A/en not_active Expired - Lifetime
- 1977-07-19 DE DE2732622A patent/DE2732622C3/de not_active Expired
- 1977-07-19 NL NL7708036A patent/NL7708036A/xx not_active Application Discontinuation
- 1977-07-22 CA CA283,370A patent/CA1074002A/en not_active Expired
- 1977-08-10 BE BE180038A patent/BE857638A/xx not_active IP Right Cessation
- 1977-08-10 SE SE7709041A patent/SE438913B/xx not_active IP Right Cessation
- 1977-09-01 FR FR7726591A patent/FR2377628A1/fr active Granted
- 1977-09-09 SU SU772519870A patent/SU689630A3/ru active
- 1977-09-26 JP JP11480177A patent/JPS5389785A/ja active Pending
- 1977-12-20 IT IT30940/77A patent/IT1088792B/it active
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1978
- 1978-01-11 GB GB1131/78A patent/GB1594891A/en not_active Expired
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Cited By (45)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4357603A (en) * | 1980-11-24 | 1982-11-02 | The United States Of America As Represented By The Depart Of Energy | Method and apparatus for acoustically monitoring the flow of suspended solid particulate matter |
WO1989004482A1 (en) * | 1987-11-02 | 1989-05-18 | Stephan Dymling | Acoustic method for measuring properties of a mobile medium |
US5056357A (en) * | 1987-11-02 | 1991-10-15 | Stephan Dymling | Acoustic method for measuring properties of a mobile medium |
US7117721B2 (en) | 1993-08-31 | 2006-10-10 | Roche Diagnostics Operations, Inc. | Fluid dose, flow and coagulation sensor for medical instrument |
US6575017B1 (en) | 1993-08-31 | 2003-06-10 | Roche Diagnostics Corporation, Inc. | Fluid dose, flow and coagulation sensor for medical instrument |
US5686659A (en) * | 1993-08-31 | 1997-11-11 | Boehringer Mannheim Corporation | Fluid dose flow and coagulation sensor for medical instrument |
US5710622A (en) * | 1993-08-31 | 1998-01-20 | Boehringer Mannheim Corporation | Fluid dose, flow and coagulation sensor for medical instrument |
US5789664A (en) * | 1993-08-31 | 1998-08-04 | Boehringer Mannheim Corporation | Fluid dose, flow and coagulation sensor for medical instrument |
WO1995006919A1 (en) * | 1993-08-31 | 1995-03-09 | Boehringer Mannheim Corporation | Method and apparatus for operating a medical instrument |
US6189370B1 (en) | 1993-08-31 | 2001-02-20 | Roche Diagnostics Corporation | Fluid dose, flow and coagulation sensor for medical instrument |
US5526111A (en) * | 1993-08-31 | 1996-06-11 | Boehringer Mannheim Corporation | Method and apparatus for calculating a coagulation characteristic of a sample of blood a blood fraction or a control |
US5824881A (en) * | 1996-09-13 | 1998-10-20 | Cobe Laboratories | Gas/fluid detector for contained fluid systems |
US20050148899A1 (en) * | 2003-10-22 | 2005-07-07 | Walker William F. | Method and apparatus for characterization of clot formation |
US9723996B2 (en) | 2003-10-22 | 2017-08-08 | Hemosonics, Llc | Method and apparatus for characterization of clot formation |
US20110034805A1 (en) * | 2003-10-22 | 2011-02-10 | Walker William F | Method and apparatus for characterization of clot formation |
US7892188B2 (en) | 2003-10-22 | 2011-02-22 | Hemosonics, Llc | Method and apparatus for characterization of clot formation |
US8740818B2 (en) | 2003-10-22 | 2014-06-03 | Hemosonics, Llc | Method and apparatus for characterization of clot formation |
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US11892459B2 (en) | 2008-12-23 | 2024-02-06 | C A Casyso Gmbh | Cartridge device for a measuring system for measuring viscoelastic characteristics of a sample liquid, a corresponding measuring system, and a corresponding method |
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US11061038B2 (en) | 2008-12-23 | 2021-07-13 | C A Casyso Gmbh | Cartridge device for a measuring system for measuring viscoelastic characteristics of a sample liquid, a corresponding measuring system, and a corresponding method |
US10996230B2 (en) | 2008-12-23 | 2021-05-04 | C A Casyso Gmbh | Cartridge device for a measuring system for measuring viscoelastic characteristics of a sample liquid, a corresponding measuring system, and a corresponding method |
US11456071B2 (en) | 2010-04-08 | 2022-09-27 | Hemosonics Llc | Hemostatic parameter display |
US10147152B2 (en) | 2010-04-08 | 2018-12-04 | Hemosonics, Llc | Hemostatic parameter display |
US10962524B2 (en) | 2011-02-15 | 2021-03-30 | HomoSonics LLC | Characterization of blood hemostasis and oxygen transport parameters |
US9031701B2 (en) | 2011-02-15 | 2015-05-12 | Hemosonics Llc | Characterization of blood hemostasis and oxygen transport parameters |
US11680940B2 (en) | 2011-02-15 | 2023-06-20 | Hemosonics Llc | Characterization of blood hemostasis and oxygen transport parameters |
US10161944B2 (en) | 2011-02-15 | 2018-12-25 | Hemosonics Llc | Methods for evaluation of hemostasis |
US9410971B2 (en) | 2011-02-15 | 2016-08-09 | Hemosonics Llc | Devices, systems and methods for evaluation of hemostasis |
US9272280B2 (en) | 2011-02-15 | 2016-03-01 | Hemosonics Llc | Device, systems and methods for evaluation of hemostasis |
US10031144B2 (en) | 2011-02-15 | 2018-07-24 | Hemosonics Llc | Devices, systems and methods for evaluation of hemostasis |
US10481168B2 (en) | 2011-02-15 | 2019-11-19 | Hemosonics Llc | Devices, systems and methods for evaluation of hemostasis |
US9977039B2 (en) | 2011-02-15 | 2018-05-22 | Hemosonics Llc | Devices, systems and methods for evaluation of hemostasis |
US11054396B2 (en) | 2011-05-19 | 2021-07-06 | Hemosonics Llc | Hemostasis analyzer |
US20160334371A1 (en) * | 2014-08-08 | 2016-11-17 | Peter Ganshorn | Method and device for determining the proportion of molecular oxygen in a respiratory gas by means of sound |
US11327069B2 (en) | 2014-09-29 | 2022-05-10 | Ca Casyso Gmbh | Blood testing system and method |
US12031993B2 (en) | 2014-09-29 | 2024-07-09 | C A Casyso Gmbh | Blood testing system and method |
US11719688B2 (en) | 2014-09-29 | 2023-08-08 | C A Casyso Gmbh | Blood testing system and method |
US11002712B2 (en) | 2015-03-17 | 2021-05-11 | Hemosonics Llc | Determining mechanical properties via ultrasound-induced resonance |
US11656206B2 (en) | 2015-03-17 | 2023-05-23 | Hemosonics Llc | Determining mechanical properties via ultrasound-induced resonance |
US10495613B2 (en) | 2015-03-17 | 2019-12-03 | Hemosonics, Llc | Determining mechanical properties via ultrasound-induced resonance |
US9726647B2 (en) | 2015-03-17 | 2017-08-08 | Hemosonics, Llc | Determining mechanical properties via ultrasound-induced resonance |
US11366093B2 (en) | 2017-04-20 | 2022-06-21 | Hemosonics, Llc | Disposable system for analysis of hemostatic function |
Also Published As
Publication number | Publication date |
---|---|
CA1074002A (en) | 1980-03-18 |
NL7708036A (nl) | 1978-07-17 |
DE2732622A1 (de) | 1978-07-20 |
SU689630A3 (ru) | 1979-09-30 |
SE7709041L (sv) | 1978-07-14 |
BE857638A (fr) | 1977-12-01 |
GB1594891A (en) | 1981-08-05 |
DE2732622B2 (de) | 1980-07-17 |
JPS5389785A (en) | 1978-08-07 |
FR2377628A1 (fr) | 1978-08-11 |
ATA483877A (de) | 1979-12-15 |
FR2377628B1 (da) | 1981-09-11 |
DE2732622C3 (de) | 1981-04-30 |
IT1088792B (it) | 1985-06-10 |
AT357807B (de) | 1980-08-11 |
CH610111A5 (da) | 1979-03-30 |
SE438913B (sv) | 1985-05-13 |
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